View genomic variant #0000023677

Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.40312930C>T
Published as -
GERP -
Segregation -
DB-ID TRIT1_000003
MSCV -
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Lishuang Shen




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
TRIT1 00003053 NM_017646.4 0000023677 ./. - - c.968G>A p.(Arg323Gln) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000584728; RCV000623099;
Chromosome 1:40312930..40312930
ClinVar Allele ID 485882
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0054742, MedGen:C4693466, OMIM:617873
ClinVar preferred disease name Inborn genetic diseases|Combined oxidative phosphorylation deficiency 35
HGVS variant names NC 000001.10:g.40312930C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA20969799|OMIM:617840.0001
Gene symbol:Gene id. TRIT1:54802
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 1047420796
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None